This invention relates to platinum co-ordination compounds, to pharmaceutical compositions containing them.
Examples of compositions falling within the scope of the present invention include:
[Pt(II)(NR 1 R2)(NR 3 R4)-(CR5 R6)(X)(Y)] or (1)
[Pt(II)(NR 1 R2)(NR 3 R4)-(CR5 R6)(CR 5 R6)(CR 7 R8)(X)(Y)] or (2)
[Pt(IV)(NR 1 R2)(NR 3 R4)-(CR5 R6)(X)(Y)(Z) 2 ] or (3)
[Pt(IV)(NR 1 R2)(NR 3 R4)-(CR5 R6)(CR 7 R8)(X)(Y)(Z) 2 ] (4)
the R groups may be the same or different and are selected from H, straight-or branched-chain alkyl, aryl, alkaryl, aralkyl, alkenyl, cydoalkyl, cycloalkenyl, halogen, pseudohalogen (as hereinafter defined), hydroxy, alkoxy, aryloxy, formyl, nitro, amido, amino, sulphonic acids or salts thereof and carboxlic esters, acids and salts thereof, or, two R groups may together represent oxygen or sulphur, and
X and Y are the same or different ligands and are selected from sulphate, phosphate, nitrate, carboxylate, substituted carboxylate and water and where R is not H or straight-chain alkyl, additionally halogen or pseudohalogen, and Z is halogen, or pseudohalogen or hydroxy.
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3. A compound selected from the group consisting of aquosulphato(N,N'-diethylethylenediamine)platinum (II) and bis(chloroacetato)-(N-ethylethylenediamine)platinum (II).
1. A coordination complex of platinum having the formula: ##STR3## in which the R groups are the same or different and are selected from H and lower alkyl and X and Y are the same or different ligands selected from sulphate, phosphate, nitrate, acetate, chloroacetate and water, provided that X and Y are not both water, such that the platinum is present as Pt(II).
2. A pharmaceutical composition comprising an effective amount of a compound according to
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This invention relates to platinum co-ordinate compounds, to pharmaceutical compositions containing them.
According to a first aspect of the invention, a composition of matter comprises a co-ordination compound of platinum having the formula
[Pt(II)(NR1 R2)(NR3 R4)-(CR5 R6) (X)(Y)] or (1)
[Pt(II)(NR1 R2)(NR3 R4)-(CR5 R6)(CR7 R8)(X)(Y)]-or (2)
[Pt(IV)(NR1 R2)(NR3 R4)(CR5 R6)(X)(Y)(Z)2 ], or (3)
[Pt(IV)(NR1 R2)(NR3 R4)-(CR5 R6)(CR7 R8)(X)(Y)(Z)2 ] (4)
in which the R groups may be the same or different and are selected from H, straight-or branched-chain alkyl, aryl, alkaryl, aralkyl, alkenyl, cycloalkyl, cycloalkenyl, halogen, pseudohalogen (as hereinafter defined), hydroxy, alkoxy, aryloxy, formyl, nitro, amido, amino, sulphonic acids or salts thereof and carboxylic esters, acids and salts thereof, or, two R groups may together represent oxygen or sulphur;
X and Y are the same or different ligands and are selected from sulphate, phosphate, nitrate, carboxylate, substituted carboxylate and water and, where R is not H or straight-chain alkyl, additionally halogen or pseudohalogen, and Z is halogen, or pseudohalogen or hydroxy.
When Z is absent, the composition of matter is a co-ordination complex of platinum (II) and has the structure: ##STR1##
When the Z groups are present, the composition is a coordination complex of platinum (IV) having the structure: ##STR2##
Where X and/or Y is represented by carboxylate or substituted carboxylate, the general formula of which is Cx R12x+1 CO2-, we prefer that x is an integer from 1 to 9 inclusive and that the R1 groups are the same or different and are selected from hydrogen, substituted or unsubstituted straight-or branched-chain alkyl, aryl, alkaryl, aralkyl, alkenyl, cycloalkyl and cycloalkenyl, halogen, pseudohalogen (as hereinafter defined), hydroxy, formyl, nitro, amido, amino and sulphonic acid salts. We intend the above definition also to include oxygen and sulphur, such that one doubly-bonded oxygen or sulphur is represented by two R1 groups.
Where X and Y are both carboxylate, they can together comprise a dicarboxylate bidentate ligand, for example oxalate and ligands having the general formula
- OOC--(CRy2 Rz3)n 1- COO-
where n1 is an integer from 2 to 6, R2 and R3 are the same or different and are selected from H, lower alkyl, aryl, alkaryl, aralkyl, alkenyl, cycloalkyl, cycloalkenyl, alkoxy, OH, halogen, pseudohalogen (as hereinafter defined)
or are combined with the carbon atoms to form a cycloalkyl or cycloalkenyl or aryl group and substituted derivatives thereof, and y and z are either 0 or 1 as long as (y+z) is equal 1 or 2.
Suitable dicarboxylate ligands are the succinato, glutarato (pentanedioato), adipato (hexanedioato), pimelato (heptanedioato), malato (cis-butenedioato) and phthalato (o-benzenedicarboxylate) ligands and these may be either substituted or unsubstituted.
The term "pseudohalogen" in this specification has the meaning given on p. 560 of "Advanced Inorganic Chemistry" by Cotton and Wilkinson, Interscience Publishers, 1966, as being "a molecule consisting of more than two electronegative atoms which, in the free state, resembles the halogens; these pseudohalogens give rise to anions which resemble the halide ions in behaviour". Examples of suitable pseudohalogens are cyanide, cyanate, thiocyanate and azide.
Normally the compound is used in association with a pharmaceutically acceptable carrier therefor. Accordingly, in a second aspect, the present invention provides a pharmaceutical composition which comprises a compound according to the first aspect of the invention and a pharmaceutically-acceptable carrier for said compound; these compositions can be formulated so as to be suitable, for example, for parenteral or oral administration.
Preparation details of complexes of platinum according to the invention will now be described by way of example.
K2 PtCl4 (50 g) in 500 ml water was filtered then KI(79 g) in 150 ml water added with stirring. N,N'-diethylethylenediamine (30 g =37.5 ml) were added. The precipitated diiodo (N,N'-diethylethylenediamine) platinum (II) was filtered off and dried in vacuo (55 g 81%). PtI2 (Et2 En) (25 g) was added to a solution of silver sulphate (13.75 g) in 200 ml of water and stirred at 50°C for three hours. The supernatant was tested to confirm that no excess silver was present, the silver iodide removed by filtration and the pale yellow liquor freeze-dried to give aquosulphato (N,N'-diethylethylenediamine) platinum (II) monohydrate.
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Assay Pt C H N S O |
______________________________________ |
Calculated |
44.03 16.25 4.51 6.32 7.22 21.67 |
Found -- 16.05 4.53 6.35 -- -- |
______________________________________ |
PREPARATION OF BIS(CHLOROACETATO)(N-ETHYLETHYLENEDIAMINE) PLATINUM (II) |
Pt(ClCH2 CO2)2 (N-ET EN) (N-ET EN=N-ETHYLETHYLENEDIAMINE) |
PtI2 (N-ET en) was prepared by Dhara's method using a 10% excess of amine. The product was washed with water (3×100 ml) and ethanol and dried in vacuo at 50°C
Yield=157.1 g (94.6%)
PtI2 (N-Et en) (50 g, 0.093 mol) was added portionwise to a stirred solution of silver nitrate (31.3 g, 0.184 mol) in water at 40°C and in the absence of light.
The mixture was stirred at 40°C for three hours, treated with charcoal and filtered through a porosity four sinter. The yellow filtrate was found to be free from excess silver on testing with NaCl.
Chloroacetic acid (19.4 g, 0.205 mol) was added to a stirred solution of the N-ethylethylenediamine diaquo complex (0.92 mol). The solution was adjusted to pH 5-6 with potassium hydoroxide, and then warmed to give a pale yellow precipitate. The mixture was stirred overnight and the solid filtered off, washed with water (20 ml), ethanol (25 ml) and dried in vacuo at 60°C for four hours.
Crude yield=35.0 g (80%)
The crude product was recrystallized from 600 ml of boiling water.
Yield of recrystallized product=20.4 g
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Assay: Pt C H N O Cl |
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Calculated % |
41.5 20.4 3.4 6.0 13.6 15.1 |
Found % -- 19.7 3.5 5.9 -- -- |
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Further compositions according to the invention include those where all the R groups are H, for example: bis (acetato)(ethylene diamine) Pt (II), aquosulphato (ethylenediamine) Pt (II) and transdihydroxy aquochloracetato (ethylenediamine)Pt(IV), those where R1 to R4 are carboxylate, for example, aquosulphato - N,N,N',N'-tetraacetatoethylenediamine Pt(II) and aquophosphato-N,N,N'N'-tetraacetato ethylene diamine Pt(II), and those where one of the R1 and R4 groups is an aryl group, for example: bis(chloroacetato)-N-phenethylenediamine (Pt(II). Furthermore, an example of a compound where X and Y are halogen is: bis-chloro(N,N,N',N'-tetracetato ethylene diamine) Pt(II).
Watkins, David M., Hydes, Paul D.
Patent | Priority | Assignee | Title |
4359425, | Apr 30 1980 | SHIONOGI & CO LTD | Organo-platinum complex |
4431666, | Mar 01 1980 | NEDERLANDSE CENTRALE ORGANISATIE VOOR TOEGEPASTNATUURWETENSCHAPPELIJK ONDERZOEK | Platinum(IV)-diamine complexes, a process for the preparation thereof, a process for the preparation of a medicine using such a platinum(IV)-diamine complex for the treatment of malignant tumors in mice |
4477387, | Jul 05 1980 | Otsuka Chemical Co., Ltd. | Platinum(II) complexes |
4482569, | Jan 03 1980 | Nederlandse Centrale Organisatie Voor Toegepastnatuurweten-Schappelijk | Platinum (IV)-diamine complexes, a process for the preparation of pharmaceutical compositions and a method of treating malignant tumors in mice |
4500465, | Jun 28 1982 | Engelhard Corporation | Solubilized platinum (II) complexes |
4533502, | Feb 22 1983 | Platinum (II) compounds and their preparation | |
4560781, | Dec 21 1982 | Shionogi & Co., Ltd. | Glycolic acid platinum complexes |
4562275, | Mar 23 1984 | WADLEY INSTITUTES OF MOLECULAR MEDICINE; KHAN, AMANULLAH | Antitumor platinum complexes |
4565884, | May 10 1983 | Andrulis Research Corporation; ANDRULIS RESEARCH CORPORATION, 7315 WISCONSIN AVENUE, BETHESDA, MN 20814 | Bis-platinum complexes as antitumor agents |
4577038, | Jun 01 1983 | Shionogi & Co., Ltd. | Glycolic acid type platinum complexes |
4598091, | Feb 18 1983 | SCHONENBERGER, HELMUT | (1,2-diphenyl)-ethylenediamine)-platinum (II) complex compounds |
4675336, | Jun 26 1985 | American Cyanamid Company | Platinum complexes of amines with dibasic acids |
4704464, | Feb 23 1985 | ASTA-WERKE AKTIENGESELLSCHAFT CHEMISCHE FABRIK, ARTUR-LADEBECK-STRASSE 128 - 152, D-4800 BIELEFELD 14, GERMANY, A CORP OF GERMANY | Tumor retarding (1-benzyl-ethylenediamine)-platin (II)-complexes |
4720504, | May 10 1983 | Andrulis Research Corporation | Use of bis-platinum complexes as antitumor agents |
4730068, | Feb 23 1985 | HELMUT, SCHONENBERGER | Tumor retarding (1,2-diphenyl-ethylenediamine)-platinum(II)-complexes |
4730069, | Sep 03 1984 | Behringwerke Aktiengesellschaft | Cis-platinum complexes with a pentaerythritol derivative as the ligand, a process for their preparation and a pharmaceutical agent containing these compounds |
4732893, | Aug 03 1984 | BOEHRINGER MANNHEIM ITALIA S P A | Amino-anthracenediones-platinum complexes useful as anticancer compounds |
4737589, | Aug 27 1985 | Nippon Kayaku Kabushiki Kaisha | Platinum Complexes |
4797393, | Jul 25 1986 | UNIVERSITY OF VERMONT AND STATE AGRICULTURAL COLLEGE, THE | Bis-platinum complexes as chemotherapeutic agents |
4861905, | Feb 19 1987 | Nippon Kayaku Kabushiki Kaisha | Platinum complexes |
4864043, | Aug 27 1985 | Nippon Kayaku Kabushiki Kaisha | Platinum complexes |
4866092, | Jun 26 1985 | American Cyanamid Company | Platinum complexes of amines with novel dibasic acids |
4871729, | Jul 25 1986 | University of Vermont and State Agricultural College | Bisplatinum complexes as chemotherapeutic agents |
4921984, | Aug 27 1985 | Nippon Kayaku Kabushiki Kaisha | Novel platinum complexes |
5068376, | Aug 27 1985 | Nippon Kayaku Kabushiki Kaisha | Novel platinum complexes |
5128493, | Feb 19 1987 | Nippon Kayaku Kabushiki Kaisha | Platinum complexes |
5380897, | May 25 1993 | Tri(platinum) complexes | |
5409915, | Sep 14 1993 | Boehringer Mannheim | Bis-platinum (IV) complexes as chemotherapeutic agents |
6322992, | Sep 01 1995 | Johnson & Johnson Clinical Diagnostics, Inc. | Method for the determination of a specific binding ligand using a vanadium bromoperoxidase as a signal-generating enzyme |
7176327, | Aug 27 2002 | UNIVERSITY COURT OF THE UNIVERSITY OF EDINBURGH, THE | Photoreactive compounds and compositions |
Patent | Priority | Assignee | Title |
4115418, | Sep 02 1976 | Government of the United States of America | 1,2-Diaminocyclohexane platinum (II) complexes having antineoplastic activity |
4119653, | Apr 06 1976 | Johnson Matthey Public Limited Company | Co-ordination compounds of platinum |
4119654, | Feb 26 1976 | Johnson Matthey Public Limited Company | Compositions containing platinum |
4137248, | Aug 29 1977 | The United States of America as represented by the Department of Health, | Compound, 4-carboxyphthalato(1,2-diaminocyclohexane)-platinum(II) and alkali metal salts thereof |
4140707, | Jun 08 1972 | RESEARCH CORPORATION TECHNOLOGIES, INC , 6840 EAST BROADWAY BLVD , TUCSON, AZ 85710 A NOT-FOR-PROFIT, NON-STOCK CORP OF DE | Malonato platinum anti-tumor compounds |
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